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"Eye Care" ophthalmic excimer laser system - Taiwan Registration c1b0b3f0c62f61f058f878f999f1324d

Access comprehensive regulatory information for "Eye Care" ophthalmic excimer laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c1b0b3f0c62f61f058f878f999f1324d and manufactured by AMO MANUFACTURING USA, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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c1b0b3f0c62f61f058f878f999f1324d
Registration Details
Taiwan FDA Registration: c1b0b3f0c62f61f058f878f999f1324d
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Device Details

"Eye Care" ophthalmic excimer laser system
TW: โ€œ็œผๅŠ›ๅฅโ€็œผ็ง‘ๆบ–ๅˆ†ๅญ้›ทๅฐ„็ณป็ตฑ
Risk Class 3

Registration Details

c1b0b3f0c62f61f058f878f999f1324d

DHA00602012301

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.0001 ็œผ็ง‘็”จๆบ–ๅˆ†ๅญ้›ทๅฐ„็ณป็ตฑ

import

Dates and Status

Aug 18, 2009

Aug 18, 2029